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United States Patent |
5,141,668
|
Nishiyama
,   et al.
|
August 25, 1992
|
Naphthalene compound and liquid crystal composition containing the same
Abstract
A naphthalene compound having the following formula (I) and a liquid
crystal composition containing the same:
##STR1##
wherein X represents a hydrogen atom or a halogen atom, Y and Z
independently represent a monovalent group selected from the group
consisting of
##STR2##
wherein W represents a hydrogen atom or a halogen atom, R represents an
alkyl group having 6 to 18 carbon atoms, provided that Y and/or Z
represent the alkyl group, which is an optically active group including an
asymmetric carbon having the following formula (II):
##STR3##
wherein A is a group or atom selected from the group consisting of alkyl
groups, alkoxy groups, halogen atoms and fluoroalkyl groups, n is an
integer of 0 to 3, m is an integer of 3 to 6, and *C represents an
asymmetric carbon.
Inventors:
|
Nishiyama; Shinichi (Ichihara, JP);
Yamaoka; Hideo (Ichihara, JP);
Yamanaka; Tooru (Ichihara, JP)
|
Assignee:
|
Mitsui Petrochemical Industries Ltd. (Tokyo, JP)
|
Appl. No.:
|
347750 |
Filed:
|
May 5, 1989 |
Foreign Application Priority Data
| May 12, 1988[JP] | 63-115093 |
Current U.S. Class: |
252/299.62; 252/299.1; 560/80; 560/85 |
Intern'l Class: |
C09K 019/32; C09K 019/52; C07C 069/76 |
Field of Search: |
252/299.01,299.6,299.61,299.62
560/100,54,59,63,65,83,85,86
|
References Cited
U.S. Patent Documents
4119558 | Oct., 1978 | Coates et al. | 252/299.
|
4820839 | Apr., 1989 | Krause et al. | 544/316.
|
4846998 | Jul., 1989 | Pohl et al. | 252/299.
|
4867904 | Sep., 1989 | Krause et al. | 252/299.
|
4871471 | Oct., 1989 | Krause et al. | 252/299.
|
4873019 | Oct., 1989 | Krause et al. | 252/299.
|
4904752 | Feb., 1990 | Kanoe et al. | 528/97.
|
4921632 | May., 1990 | Nakamura et al. | 252/299.
|
4973738 | Nov., 1990 | Suzuki et al. | 560/80.
|
Foreign Patent Documents |
294852 | Dec., 1988 | EP.
| |
332456 | Sep., 1989 | EP.
| |
0339987 | Nov., 1989 | EP.
| |
339987 | Nov., 1989 | EP.
| |
62-10045 | Jan., 1987 | JP.
| |
63-246346 | Oct., 1988 | JP.
| |
1-128954 | May., 1989 | JP.
| |
8706577 | Nov., 1987 | WO.
| |
Primary Examiner: Stoll; Robert L.
Assistant Examiner: Wu; Sheam C.
Attorney, Agent or Firm: Nixon & Vanderhye
Claims
We claim:
1. A naphthalene compound of the formula (I):
##STR39##
wherein A represents CF.sub.3, n is an integer of 1 to 3, m is an integer
of 3 to 6 is an integer of 6 to 18 .
2. A liquid crystal composition comprising a naphthalene compound as
claimed in claim 1.
Description
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a novel naphthalene compound and a liquid
crystal composition containing the same. More specifically, the present
invention relates to a novel naphthalene compound having an optically
active group and a liquid crystal composition containing the same.
2. Description of the Related Art
In the prior art, CRT devices are most frequently used as display devices
for OA instruments, and in the field of instruments having display devices
such as OA instruments, there is an increasing demand for a
miniaturization and reduction of the weight of these instruments, or an
enlargement of the picture area and a reduced thickness of the picture
unit of the display devices. Accordingly, to meet the respective usages
and demands the CRT devices of the prior art have been replaced by various
newly developed display devices, for example, liquid crystal display,
plasma display, LED display, EL display, and ECD display devices.
Among these display devices, the liquid crystal display device sends
electric signals to a switching element basically by using a liquid
crystal compound to change the state of the liquid crystal compound in the
switching element, to thereby control the shielding and transmission of
light to elicit electric signals, and is practically applied not only as a
display device for the OA instruments as mentioned above, but also as a
display device for digital watches or portable games, etc., and further,
is now used as a display device for moving pictures, such as for a small
television receiver.
In the display device using a liquid orystal compound as described above,
various drive systems are known, for example, the TN (twist nematic) mode
is used as the drive system for current liquid crystal display devices.
The TN mode is a system which obtains a display by utilizing the
dielectric anisotropy of the molecules in the nematic phase of the liquid
crystal compound, whereby the display device is driven by the energy in
proportion to the square of the electrical field externally applied
(f.alpha.E.sup.2).
In switching elements employing this system, however, to change the
displayed picture the position of the molecules of the liquid crystal
compound must be changed, and therefore, the drive time is prolonged and a
problem arises in that the voltage required for changing the molecule
position of the liquid crystal compound, namely the consumption power,
becomes greater. In such a switching element, since the switching
threshold value characteristic is poor, when switching actuation is
attempted by changing the molecular position at a high speed, a leak
voltage occurs even at non-display picture portions, whereby the display
contrast is often remarkably lowered.
Accordingly, the display system using the TN mode of the prior art is not
always an appropriate display device system for displaying moving
pictures, particularly as a display device having a large picture area or
for a miniature digital television receiver.
A display device utilizing STN (super twist nematic) having an improved
switching threshold value characteristic as the TN mode is also used, and
by utilizing the STN mode, the switching threshold value characteristic
can be improved, and thus the contrast of the display device can be
improved. Nevertheless, this method is the same as the TN mode in that it
utilizes a dielectric anisotropy, and therefore, the switching time is
prolonged and the same tendency as that of the display device utilizinq
the TN mode is exhibited when it is used as a display device for moving
pictures, particularly a display device having a large picture area or for
a miniature digital television receiver.
Conversely, the organic compound synthesized by R. B. Meyer et al, in 1975
exhibited a ferroelectric property, and further, in 1980 R. B. Meyer
suggested the use of a ferroelectric liquid crystal compound as the
optical switching element, namely the display device, by filling these
ferroelectric liquid crystal compounds in a cell with a small gap.
The switching element using the ferroelectric liquid crystal compound as
described above, different from the switching element utilizing the TN
mode or the STN mode, functions as a switching element only by changing
the alignment direction of the molecules of the liquid crystal compound,
whereby the switching time is greatly reduced. Further, since the value of
Ps.times.E given by the spontaneous polarization (Ps) possessed by the
ferroelectric liquid crystal compound and the electrical field intensity
(E) is the effective energy strength for changing the direction of
alignment of the molecules of the liquid crystal compound, the consumption
power is also greatly reduced. Such a ferroelectric liquid crystal
compound has two stable states, depending on the direction of the applied
electrical field, namely has bistability, and a good switching threshold
characteristic, and therefore is particularly suitable as a display device
for moving pictures.
When such a ferroelectric liquid crystal compound is used for the optical
switching element, the ferroelectric liquid crystal compound must have
characteristics such as an actuation temperature range near normal
temperature, a wide actuation temperature width, and a high switching
speed and switching threshold value voltage within a required range.
Especially, the actuation temperature range is very important when using a
ferroelectric liquid crystal compound, and the actuation temperature range
does not coincide with the service temperature range in many ferroelectric
liquid crystal compounds, although the other characteristics may be very
good (see, for example, R. B. Meyer et al, J. de Phs., vol. 36 L-p.69,
1975).
Further, in the pre-text of the llth Liquid Crystal Discussion, p. 16
(1985) reported by Mr. Masaaki Taguchi and Mr. Takamasa Harada or in
Japanese Unexamined Patent Publication (Kokai) No. 62-10045, for example,
ferroelectric liquid crystal compounds having a naphthalene ring are
disclosed. The liquid crystal compounds disclosed have a relatively higher
practical applicability from the view point of the actuation temperature
range, but they do not satisfy all of the other characteristic
requirements for a ferroelectric liquid crystal compound, and there is
still room for an improvement thereof.
SUMMARY OF THE INVENTION
Accordingly, the object of the present invention is to provide a novel
naphthalene compound which can be used as the liquid crystal compound.
Another object of the present invention is to provide a novel liquid
crystal composition which can form a display device having excellent
characteristics.
A further object of the present invention is to provide a novel liquid
crystal composition capable of forming an element having excellent
characteristics such as an actuation temperature range near normal
temperature, a wide actuation temperature width, a high switching speed,
and a switching threshold value voltage within a required range.
Other objects and advantages of the present invention will be apparent from
the following description.
In accordance with the present invention, there is provided a naphthalene
compound having the following formula (I), preferably (I'):
##STR4##
wherein X represents a hydrogen atom or a halogen atom, Y and Z
independently represent a monovalent group selected from the group
consisting of
##STR5##
wherein W represents a hydrogen atom or a halogen atom, R represents an
alkyl group having 6 to 18 carbon atoms, provided that at least one group
of y and Z represents the alkyl group, which is an optically active group
including an asymmetric carbon having the following formula (II):
wherein A is a group or atom selected from the group consisting of alkyl
groups, alkoxy groups, halogen atoms and fluoroalkyl groups, n is an
integer of 0 to 3, m is an integer of 3 to 6, and *C represents an
asymmetric carbon. The term "fluoroalkyl group" used herein means an alkyl
group, in which at least one hydrogen atom is substituted with fluorine
atom. Example of such a group is trifluoroomethyl (--CF.sub.3),
monofluoromethyl (--CFH.sub.2) or lthe like.
In accordance with the present invention, there is also provided a liquid
crystal composition which comprises a naphthalene compound having the
following formula (i), preferably (I'):
##STR6##
wherein X represents a hydrogen atom or a halogen atom, Y and Z each
independently represent a monovalent group selected from the group
consisting of
##STR7##
wherein W represents a hydrogen atom or a halogen atom, R represents an
alkyl group having 6 to 18 carbon atoms, and the alkyl group consisting at
least one alkyl group of Y and Z is an optically active group including an
asymmetric carbon having the following formula (II):
##STR8##
wherein A is a group or atom selected from the group consisting of alkyl
groups, alkoxy groups, halogen atoms and fluoroalkyl groups, n is an
integer of 0 to 3 , m is an integer of 3 to 6 , and *C represents an
asymmetric carbon.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The naphthalene compound according to the present invention exhibits the
smectic phase at around room temperature, because an alkyl group having 4
to 7 carbon atoms is attached to the optically active carbon.
Therefore, the liquid crystal composition containing a naphthalene compound
exhibiting the smectic phase at such a low temperature is practically
valuable, since the liquid crystal service temperature is within the
required range.
The naphthalene compound according to the present invention has the
following formula (I), preferably (I'):
##STR9##
wherein X represents a hydrogen atom or a halogen atom, Y and Z
independently represent a monovalent group selected from the group
consisting of
##STR10##
wherein W represents a hydrogen atom or a halogen atom, R represents an
alkyl group having 6 to 18 carbon atoms, and the alkyl group constituting
at least one alkyl group of Y and Z is an optically active group including
an asymmetric carbon having the following formula (II):
##STR11##
wherein A is a group or atom selected from the group consisting of alkyl
groups, preferably those havving 1 to 10 carbon atoms, alkoxy groups,
preferably those havving 1 to 10 carbon atoms, halogen atoms (e.g., Cl,
Br, I), and fluoroalkyl groups, preferably those having 1 to 10 carbon
atoms, and in the above formula (II), n is an integer of 0 to 3,
preferably 0 to 1, and m is an integer of 3 to 6, preferably 4 to 5.
Therefore, the naphthalene compounds where m is 0 to 2 are not included in
the present invention. Since mis the formula (II) is 3 to 6 according to
the present invention, the liquid crystal temperature exists near normal
temperature and extends a wide range. In the above-mentioned formula (II),
*C represents an asymmetric carbon.
Therefore, in the above-mentioned formula (II), the group represented by A
cannot be the same as the group represented by --(CH.sub.2).sub.m
--CH.sub.3. The group A in the formula (II) is preferably a fluoroalkyl
group of alkyl group in the present invention. Especially preferable alkyl
group is an ethyl group.
Examples of the napthalene compound according to the present invention
represented by the above-mentioned formula (II) are those represented by
the following formulae (1) to (49).
##STR12##
In the above-mentioned formulae (1) to (49), X and W are each either a
hydrogen atom or a halogen atom, each of R.sup.1 and R.sup.2 represents an
alkyl group having 1 to 18 carbon atoms, and either one of R.sup.1 and
R.sup.2, or both of R.sup.1 and R.sup.2, represent a group having an
asymmetric carbon (*C) having the following formula (II):
##STR13##
In the above-mentioned formula (II), A is either a group or atom of alkyl
groups, alkoxy groups, halogen atoms and fluoroalkyl groups, n is an
integer of 0 to 3, preferably 0 to 1, m is an integer of 3 to 6,
preferably 4 to 5, and *C represents an asymmetric carbon.
The compounds particularly preferable as liquid crystal compounds are those
having the formula (3), and specifically, the compounds having the
following formula (3-a) are particularly preferred.
##STR14##
In the above-mentioned formula [3-a], l is an integer of 1 to 18, n is an
integer of 0 to 3, m is an integer of 3 to 6, and A is either a group or
atom of alkyl groups, alkoxy groups, halogen atoms and fluoroalkyl groups:
*C represents an asymmetric carbon.
The naphthalene compound of the present invention can be prepared by
utilizing known synthetic techniques.
For example, the compounds represented by the above-mentioned formula (3-a)
can be synthesized by following the synthesizing route shown below.
##STR15##
In the above-mentioned formulae, m, n, A, and l are the same as defined
above.
More specifically, 4-benzyloxybenzoic acid (III) is reacted with a
chlorinating agent such as thionyl chloride in the presence of pyridine to
obtain a 4-benzyloxybenzoic acid chloride (IV), which compound (IV) is
reached with an alcohol compound having the formula (V) to obtain a
compound (VI). The compound (VI) is reduced by hydrogen gas, in the
presence of a catalyst such as palladium-carbon, to carry out a
debenzylation reaction and obtain a compound (VII).
Separately, 6-alkoxy.-2-carboxynaphthalene (VIII) is prepared, and the
compound (VIII) is reacted with a chlorinating agent such as thionyl
chloride to obtain a compound (IX).
Subsequently, by reacting the above-mentioned compound (VII) with the
compound (IX) in the presence of pyridine, the final compound (3-a) can be
obtained.
In order that the compound having the formula (3-a) may have optical
activity, as the alcohol compound (V), for example, there are included
4-undecanol, 3-decanol, 2-nonanol, 3-nonaol, 2-octanol, 3-octanol,
1-chlorooctanol, 1-fluorooctanol, 1,1,1-trichloro-2-octanol,
1,1,1-trifluoro-2-octanol, 2-heptanol, 3-heptanol, 1-chloroheptanol,
1-fluoroheptanol, 1,1,1-trichloro2-heptanol, 1,1,1-trifluoro-2-heptanol,
2-hexanol, 1-chlorohexanol, 1-fluorohexanol, 1,1,1-trichloro-2-hexanol,
1,1,1-trifluoro-2-hexanol, 1-chloropentanol, 1-fluoropentanol.
The naphthalene compound has the naphthalene skeleton at the core portion
of the molecule, and therefore, has a specific feature in that the
molecule itself has a certain rigidity and that the cohesive force of the
molecule as a whole is small.
There are many compounds among such naphthalene compounds which can be used
as ferroelectric liquid crystal compounds in switching elements for
controlling light transmissivity by, for example, permitting a
ferroelectric liquid crystal compound to be interposed between opposed
electrodes or magnetic poles and changing the tilt angle of the
ferroelectric liquid crystal compound. More specifically, the
ferroelectric liquid crystal compound to be used as such a switching
element must have the smectic phase at around room temperature, and a
value of the spontaneous polarization in the smectic phase (Ps) and a
viscosity coefficient within required ranges. Therefore, among the
naphthalene compounds mentioned above, the compounds exhibiting the
smectic phase can be used as the main agent of the smectic liquid crystal
composition to be used as the ferroelectric liquid crystal composition or
as the aid for the liquid crystal composition using other compounds
exhibiting the smectic phase as the main agent.
Typical examples of such compounds include the compounds having the
following formula (X).
Of these compounds, the phase transition point exhibited by the compound
having the following formula (X) is shown in the following Table 1. In the
Table, C (or Cry) indicates a crystal phase, SmA a smectic A phase, SmC a
smectic C phase, Iso an isotropic liquid, and the numerals of the
respective phases having the mark * indicate the transfer temperatures
from that phase to the phase written on the right thereof.
TABLE 1
______________________________________
##STR16## (X)
Compound C SmC SmA Iso
______________________________________
[X] Temperature * 60.degree. C.*
elevation
Temperature * 20.degree. C.*
60.degree. C.*
drop
______________________________________
As is clear from Table 1, the naphthalene compound has the smectic phase at
a temperature around room temperature or lower than room temperature. In
the prior art, a large number of liquid crystal compounds having the
smectic phase are known, but a compound substantially exhibiting the
smectic phase alone at a temperature of 30.degree. C or lower is not
known.
For example, the compound having the naphthalene skeleton represented by
the following formula (XI):
##STR17##
wherein the alkyl group bonded to optically active carbon *C is a propyl
group, exhibits a liquid crystal phase at 50.degree. C or higher, and does
not exhibit a liquid crystal phase at a lower temperature.
In contrast, the naphthalene compound of the present invention wherein the
alkyl group bonded to the optically active carbon *C is a butyl, pentyl,
hexyl or heptyl group exhibits the smectic phase at a low temperature
(e.g. 20.degree. C) which cannot be obtained with the naphthalene
compounds of the prior art.
Therefore, the naphthalene compound of the present invention can be used
alone as the liquid crystal compound or as a mixture with another liquid
crystal compound, as long as the liquid crystal phase temperature range of
the other liquid crystal compound can be lowered to around room
temperature.
The liquid crystal composition will now be described.
The liquid crystal composition of the present invention contains the
naphthalene compound represented by the above-mentioned formula (I).
In the liquid crystal composition of the present invention, the content of
the compound represented by the above-mentioned formula (I) can be as
required in view of the characteristics of the substituted naphthalene
compound used, the viscosity of the composition, the actuation
temperature, and the use thereof.
In the liquid crystal composition according to the present invention,
examples of the compounds exhibiting the chiral smectic C phase which can
be formulated together with the liquid crystal compound represented by the
formula (I) include (+)-4'-(2"-methylbutyloxy)
phenyl-6-octyloxy-napthalene-2- carboxylic acid ester,
4'-decyloxyphenyl-6-((+)-2"-methylbutyloxy) naphthalene-2-carboxylic acid
ester,
##STR18##
Further, examples of compounds other than the compounds exhibiting the
chiral smectic C phase, which can be formulated with the substituted
naphthalene compound having the formula (I) as described above to
constitute the liquid crystal composition of the present invention include
nematic liquid crystal compounds typically represented by Schiff base type
liquid crystal compounds such as:
##STR19##
azoxy type liquid crystal compounds such as:
##STR20##
benzoic acid ester type liquid crystal compounds such as:
##STR21##
cyclohexylcarboxylic acid ester type liquid crystal compounds such as:
##STR22##
biphenyl type liquid crystal compounds such as:
##STR23##
terphenol type liquid crystal compounds:
##STR24##
cyclohexyl type liquid crystal compounds:
##STR25##
and pyridine type liquid crystal compounds such as;
##STR26##
and further, cholesteric type liquid crystal compounds such as
cholesterine hydrochloride, cholesterine nonanooate, and cholesterine
oleate, and known smectic liquid crystal compounds.
The liquid crystal composition according to the present invention may also
contain additives which can be formulated in conventional liquid crystal
compositions, such as an electroconductivity imparting agent and life
enhancer.
As examples of the display method using the liquid crystal composition of
the present invention, the following methods may be specifically employed.
In the first method a display is effected by utilizing two polarizing
plates and birefringence of a ferroelectric liquid crystal compound, in
which the liquid crystal composition is injected into a thin film cell
having a gap of, for example, 2 to 5 .mu.m, the ferroelectric compound is
aligned in parallel to the substrate by utilizing the regulating force of
the substrate, interposing the thin film cell having the liquid crystal
composition injected therein between two polarizing plates, and an
external electrical field is applied to the thin film cell, to thereby
change the alignment vector of the ferroelectric liquid crystal compound.
The electrode to be used in this case preferably has silica obliquely
vapor-deposited thereon.
The second method utilizes the bichrome characteristic by mixing the liquid
crystal composition of the present invention with a bichrome dye, and in
this method a display is effected by changing the absorption of light with
the dye by changing the direction of alignment of the ferroelectric liquid
crystal composition. The dye to be used in this case is generally a
bichrome dye, and examples of such a bichrome dye include azo dyes,
naphthoquinone type dyes, cyanine type dyes, and anthraquinone type dyes.
The liquid crystal composition according to the present invention also can
be employed according to a display method conventionally utilized, other
than the above-mentioned display methods.
The display device produced by using the liquid crystal composition can be
driven by drive systems for electrical address display, optical address
display, heat address display, and electron beam address, including a
static drive, a simple matrix drive, and a composite matrix drive.
Due to the presence of an alkyl group having 4 to 7 carbon atoms bonded to
an optically active carbon, the naphthalene compound according to the
present invention exhibits the smectic phase at around room temperature,
and therefore, the liquid crystal composition containing a naphthalene
compound exhibiting the smectic phase at such a low temperature is
advantageous because the liquid crystal service temperature is within a
required range.
Also, the liquid crystal composition containing the naphthalene compound as
described above has a value of spontaneous polarization and a viscosity
coefficient within required ranges, and therefore, in the display method
using the smectic liquid phase composition, a high speed response of some
10 .mu.sec or lower can be obtained. Therefore, by using the smectic
liquid crystal composition as the switching element for a display device
having a large picture area with a large number of scanning lines, due to
the short time required for each scanning, a display of large picture area
having a sharp contrast can be obtained.
Also, by preparing a thin film cell by using the smectic liquid crystal
composition and forming the smectic phase within the thin layer cell, due
to the spontaneous polarization possessed by the liquid crystal compound,
the thin layer cell can act as a memory, and thus a continuous application
of voltage is not required and a reduction in the power consumed for the
display can be obtained. Further, in this case, the contrast becomes very
sharp.
The switching element using the smectic liquid crystal composition can be
switched only by changing the direction of alignment of the molecules, and
the primary item of electrical field intensity acts on the drive, whereby
a low voltage primary drive can be obtained.
Accordingly, of the liquid crystal compositions provided by the present
invention, by using the smectic liquid crystal composition, a display for
a large picture area having a lower consumption power and sharper contrast
can be produced.
Further, due to the short drive time and low drive voltage, the composition
also can be used as a switching element for a display device for moving
pictures.
EXAMPLES
The present invention will now be further illustrated by, but is by no
means limited to, the following Examples.
EXAMPLE 1
Synthesis of
2-[4'(R-1"-methylheptylcarbonyl)-phenyloxy]-6-decyloxynaphthalene
##STR27##
First step
Amounts of 11.4 g (50 mmole) of 4-benzyloxybenzoic acid, 36.6 ml (0.5 mole)
of thionyl chloride, and 0.1 ml of DMF were mixed and stirred at
70.degree. C for 2 hours, followed by heating under reflux for one hour.
After the refluxing, unreacted thionyl chloride was obtained to give
4-benzyloxybenzoic acid chloride of the desired product.
Second step
An amount of 12.3 g (50 mmole) of 4-benzyloxybenzoic acid chloride obtained
in the first step was dissolved in 100 ml of THF, and separately, a
mixture of 6.5 g (50 mmole) of R-2-octanol and 60.4 ml (0.75 mmole) of
pyridine was prepared, and the above THF solution of 4-benzyloxybenzoic
acid chloride was added dropwise to the mixture while stirring.
After the dropwise addition, stirring was continued for 24 hours, and
thereafter, the reaction mixture was thrown into water and the reaction
product was extracted with ether.
From the ether solution obtained, ether was removed and the residue
obtained was recrystallized by a hexane solvent to obtain 12.84 g (37.8
mmole) of 1'-methylheptyloxy-4-benzyloxybenzoate of the desired product.
Third step
Amounts of 12.84 g (37.8 mmole) of 1'-methylheptyl-oxy-4-benzyloxybenzoate,
2.49 g of carbon having 5% weight of palladium carried thereon, and 150 ml
of ethanol were mixed, and hydrogen gas was bubbled therein under normal
pressure for 8 hours.
Subsequently, the reaction mixture was filtered to remove the catalyst, and
the filtrate was concentrated to obtain 9.57 g (37.8 mmole) of
1-methylheptyloxy-4-hydroxybenzoate.
Fourth step
Separately, 0.66 g (2 mmole) of 6-decyloxy-2-carboxy-naphthalene was mixed
with 1.5 ml (20 mmole) of thionyl chloride and 0.02 ml of DMF and stirred
at 70.degree. C for 2 hours, followed by heating under reflux for 1 hour.
Subsequently, by removing unreacted thionyl chloride,
6-decyloxynaphthalene-2-carboxylic acid chloride of the desired product
was obtained.
Fifth step
Amounts of 0.69 g (2 mmole) of 6-decyloxynaphthalene-2-carboxylic acid
chloride, 0.6 g (4 mmole) of 1'-methylheptyloxy-4-hydroxybenzoate, and
2.41 ml (30 mmole) of pyrinde were added to 20 ml of THF and stirred at
40.degree. C for 3 hours, followed by throwing the reaction mixture into
water.
The reaction product was extracted with ether, washed with water, and
concentrated.
The concentrate obtained was separated by column chromatography to obtain
0.56 g of
2-[4'(R-1"-methylheptylcarbonyl)phenyloxy]-6-decyloxy-naphthalene of the
final product. .sup.1 H-NMR of the compound obtained was measured. .sup.1
H-NMR (270 MHz, CDCl.sub.3)
.delta.(ppm) 0.8-1.0 (m, 9H, --CH.sub.3)
1.2-2.0 (m, 26H)
4.0-4.2 (t, 2H, --O--CH.sub.2 --)
5.1-5.2 (d, 1H, --O--CH--)
7.2-8.2 (m, 10H, aromatic)
From the above 1H-NMR results, the compound obtained was confirmed to be
2-[4'(R-1"-methylheptylcarbonyl)phenyloxy]6-decyloxynapthalene.
The phase transition temperatures of this compound are shown as follows:
##STR28##
EXAMPLE 2
Synthesis of
2-[4'(R-1"-trifluoromethylheptyloxycarbonyl]-6-decyloxynaphthalene
##STR29##
The desired compound was obtained in the form of a white solid powder in
the same manner as in Example 1, except that 1,1,1-trifluoro-R-2-octanol
was used instead of the R-2-octanol. From the mass spectrum data, i.e.,
MS: M/e=614(P), it was confirmed that the desired compound was obtained.
The phase transition temperatures of this compound are shown as follows:
##STR30##
This compound possesses a wider liquid crystal temperature range extending
from room temperature to a lower temperature side, when compared with
2-[4'(R-2"-methylbutyloxycarbonyl)phenyloxycarbonyl]-6-decyloxynaphthalene
disclosed in Japanese Unexamined Patent Publication (Kokai) No. 62-10045:
##STR31##
having the following phase transition temperatures:
##STR32##
That is, when m is 3 to 6 in the formula (II), the liquid crystal
temperature range exists near normal temperature and extends a wider
range.
EXAMPLE 3
Synthesis of 2-4'(R-1"-ethylhexyloxycarbonyl)
phenyloxycarbonyl]-6-decyloxynaphthalene
##STR33##
The desired compound was obtained in the form of a white solid powder in
the same manner as in Example 1, except that R-3-octanol was used instead
of R-2-Octanol.
From the mass spectrum data, i.e., MS:M/e=560 (P), it was confirm that the
desired compound was obtained.
The phase transition temperatures of this compound are shown as follows.
##STR34##
EXAMPLE 4
Synthesis of 2-[6'(R-1"-methylheptyloxycarbonyl)
naphthyloxycarbonyl]-6-decyloxynaphthalene
##STR35##
The desired compound was obtained in the form of a white solid powder in
the same manner as in Example 1, except that
2-benzyloxynaphthalene-6-carboxylic acid was used instead of
4-benzyloxybenzoic acid.
From the mass spectrum data, i.e., MS:M/e=610, it was confirm that the
desired compound was obtained.
The phase transition temperatures of this compound are shown as follows.
##STR36##
EXAMPLE 5
When 11 parts by weight of the compound prepared in Example 2 was mixed
with 89 parts by weight of a known strong dielectric liquid crystal
ZLI-3488 (available from Merck & Co., Inc), the phase transition
temperatures of the resultant
mixture were as follows:
##STR37##
As is clear from the above-results, the compound prepared in Example 2 is
useful for widening the smectic liquid crystal phase. The phase transition
temperatures of the above-mentioned known strong dielectric liquid crystal
ZLI-3488 are as follows:
##STR38##
The compounds in which group A is (II) fluoroalkyl or ethyl as those
prepared in Examples 2 and 3 possess a wider liquid crystal temperature
range extending from room temperature to a lower temperature side when
compared with the compounds disclosed in Japanese Unexamined Patent
Publication (Kokai) No. 62-10045. Namely, when m is 3 to 6 in the formula
(II); the liquid crystal temperature exists near normal temperature and
extends a wider range.
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